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Real-time Videoconference-based Exercise in Eldercare Workers (ReViEEW)

A

Ander Espin

Status

Completed

Conditions

Mental Disorders
Pain

Treatments

Behavioral: Real-time videoconference-based Exercise program

Study type

Interventional

Funder types

Other

Identifiers

NCT05050526
Eldercare2021

Details and patient eligibility

About

Formal caregiving of elderly dependent people is a both physically and psychologically demanding job, and both musculoskeletal and mental disorders with a negative impact in general health and quality of life are habitual among eldercare workers. Previous research has shown that physical exercise programs can reduce and/or prevent those disorders, consequently improving well-being at work.

Online exercise interventions might be a cost-effective tool, as they can reach a large number of people at a relatively low cost. Moreover, they are compatible with situations in which interpersonal physical distancing is required, such as the current COVID-19 pandemic. However, real-time videoconference-based exercise interventions have not yet been studied in working populations.

Thus, the aim of this study is to assess the effects of a real-time videoconference-based exercise intervention in eldercare workers. The primary outcome will be low back pain. Pain in neck, shoulders and wrists/hands will also be recorded, as well as additional measures of physical fitness, psychoaffective state, health and work-related variables. All outcomes will be measured at baseline and at 12-week and 48-week follow-ups.

Enrollment

130 patients

Sex

All

Ages

18+ years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Professional eldercare workers with ≥3 months of experience in the profession
  • Employment contract at least until the anticipated date of study end

Exclusion criteria

  • Pregnancy
  • Contraindication to exercise according to the American College of Sports Medicine Guidelines

Trial design

Primary purpose

Supportive Care

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Double Blind

130 participants in 2 patient groups

Exercise program
Experimental group
Description:
Participants in the experimental group will take part in a 12-week exercise program.
Treatment:
Behavioral: Real-time videoconference-based Exercise program
Control
No Intervention group
Description:
Participants in the control group will not receive any intervention.

Trial contacts and locations

2

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Central trial contact

Ander Espin, PhD Student

Data sourced from clinicaltrials.gov

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